Marsico Lung Institute and Cystic Fibrosis Research Center, United States; Department of Cell Biology and Physiology, United States.
Marsico Lung Institute and Cystic Fibrosis Research Center, United States; Department of Pathology and Laboratory Medicine, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, United States.
Adv Drug Deliv Rev. 2023 Jul;198:114866. doi: 10.1016/j.addr.2023.114866. Epub 2023 May 15.
Epithelial cells from mucociliary portions of the airways can be readily grown and expanded in vitro. When grown on a porous membrane at an air-liquid interface (ALI) the cells form a confluent, electrically resistive barrier separating the apical and basolateral compartments. ALI cultures replicate key morphological, molecular and functional features of the in vivo epithelium, including mucus secretion and mucociliary transport. Apical secretions contain secreted gel-forming mucins, shed cell-associated tethered mucins, and hundreds of additional molecules involved in host defense and homeostasis. The respiratory epithelial cell ALI model is a time-proven workhorse that has been employed in various studies elucidating the structure and function of the mucociliary apparatus and disease pathogenesis. It serves as a critical milestone test for small molecule and genetic therapies targeting airway diseases. To fully exploit the potential of this important tool, numerous technical variables must be thoughtfully considered and carefully executed.
气道黏液纤毛部位的上皮细胞可在体外轻易地生长和扩增。当在气液界面(ALI)的多孔膜上生长时,这些细胞会形成一个连续的、电阻性的屏障,将顶端和基底外侧隔离开来。ALI 培养物复制了体内上皮组织的关键形态、分子和功能特征,包括黏液分泌和黏液纤毛转运。顶端分泌物中包含分泌凝胶形成的黏蛋白、脱落的细胞相关的黏着性黏蛋白,以及数百种参与宿主防御和内稳态的其他分子。呼吸上皮细胞 ALI 模型是一个久经考验的得力工具,已被用于各种阐明黏液纤毛装置的结构和功能以及疾病发病机制的研究。它是针对气道疾病的小分子和基因治疗的关键里程碑测试。为了充分利用这个重要工具的潜力,必须深思熟虑并仔细执行许多技术变量。